Comparative Neuroanatomy Laboratory, Department of Biology, Ecology and Earth Sciences (DiBEST), University of Calabria, Ponte Pietro Bucci 4B, Arcavacata di Rende, 87036 Cosenza, Italy.
Comparative Neuroanatomy Laboratory, Department of Biology, Ecology and Earth Sciences (DiBEST), University of Calabria, Ponte Pietro Bucci 4B, Arcavacata di Rende, 87036 Cosenza, Italy; Health Center s.r.l., 87100 Cosenza, Italy.
Exp Neurol. 2023 Aug;366:114432. doi: 10.1016/j.expneurol.2023.114432. Epub 2023 May 5.
Autism Spectrum Disorder (ASD) is increasing, but its complete etiology is still lacking. Recently, application of ketogenic diet (KD) has shown to reduce abnormal behaviors while improving psychological/sociological status in neurodegenerative diseases. However, KD role on ASD and underlying mechanism remains unknown. In this work, KD administered to BTBR T Itpr3/J (BTBR) and C57BL/6J (C57) mice reduced social deficits (p = 0.002), repetitive behaviors (p < 0.001) and memory impairments (p = 0.001) in BTBR. Behavioral effects were related to reduced expression levels of tumor necrosis factor alpha, interleukin-1β, and interleukin-6 in the plasma (p = 0.007; p < 0.001 and p = 0.023, respectively), prefrontal cortex (p = 0.006; p = 0.04 and p = 0.03) and hippocampus (p = 0.02; p = 0.09 and p = 0.03). Moreover, KD accounted for reduced oxidative stress by changing lipid peroxidation levels and superoxide dismutase activity in BTBR brain areas. Interestingly, KD increased relative abundances of putatively beneficial microbiota (Akkermansia and Blautia) in BTBR and C57 mice while reversing the increase of Lactobacillus in BTBR feces. Overall, our findings suggest that KD has a multifunctional role since it improved inflammatory plus oxidative stress levels together with remodeling gut-brain axis. Hence, KD may turn out be a valuable therapeutic approach for ameliorating ASD-like conditions even though more evidence is required to evaluate its effectiveness especially on a long term.
自闭症谱系障碍(ASD)正在增加,但它的完全病因仍不清楚。最近,生酮饮食(KD)的应用已显示出在神经退行性疾病中减少异常行为同时改善心理/社会学状态的作用。然而,KD 在 ASD 中的作用及其潜在机制仍不清楚。在这项工作中,给予 BTBR T Itpr3/J(BTBR)和 C57BL/6J(C57)小鼠的 KD 减少了 BTBR 的社交缺陷(p=0.002)、重复行为(p<0.001)和记忆障碍(p=0.001)。行为效应与血浆中肿瘤坏死因子-α、白细胞介素-1β和白细胞介素-6 的表达水平降低有关(p=0.007;p<0.001 和 p=0.023),分别在额皮质(p=0.006;p=0.04 和 p=0.03)和海马(p=0.02;p=0.09 和 p=0.03)。此外,KD 通过改变 BTBR 大脑区域的脂质过氧化水平和超氧化物歧化酶活性来解释氧化应激的减少。有趣的是,KD 增加了 BTBR 和 C57 小鼠中假定有益的微生物群落(阿克曼氏菌和布劳特氏菌)的相对丰度,同时逆转了 BTBR 粪便中乳杆菌的增加。总的来说,我们的发现表明 KD 具有多功能作用,因为它改善了炎症加氧化应激水平,同时重塑了肠道-大脑轴。因此,KD 可能成为改善 ASD 样病症的有价值的治疗方法,尽管需要更多的证据来评估其有效性,特别是在长期。